LD304 MATERNITY BED Adverse Event — Malfunction (MDR 0001831750-2020-00428)
LD304 MATERNITY BED Adverse Event — Malfunction (MDR 0001831750-2020-00428) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LD304 MATERNITY BED; Generic name: TABLE, OBSTETRICAL, AC-POWERED (AND ACCESSORIES); Manufacturer: STRYKER MEDICAL-KALAMAZOO.
| Device | LD304 MATERNITY BED |
|---|---|
| Generic name | TABLE, OBSTETRICAL, AC-POWERED (AND ACCESSORIES) |
| Manufacturer | STRYKER MEDICAL-KALAMAZOO |
| Report number | 0001831750-2020-00428 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | THIS MDR IS PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. THE DEVICE WAS EVALUATED IN THE FIELD BUT THE ISSUE WAS NOT CONFIRMED; NO DEFECT OR MALFUNCTION WAS FOUND. THERE WAS NO REMEDIAL ACTION TAKEN. THIS DEVICE IS NOT LABELED FOR SINGLE USE. |
| Source | openFDA MAUDE (device adverse events) |
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